Wang, Jie team published research in Chemical Communications (Cambridge, United Kingdom) in 2020 | 72824-04-5

72824-04-5, Allylboronic acid pinacol ester is a useful research compound. Its molecular formula is C9H17BO2 and its molecular weight is 168.04 g/mol. The purity is usually 95%.
Allylboronic acid pinacol ester is an allylation reagent that is used to produce aldehydes from ketones. It reacts with water, yielding the desired product and formaldehyde as a byproduct. The reaction proceeds through a sequence of steps, in which the boronate ester first reacts with water to form an allylboronate ion and hydrogen gas. This intermediate then reacts with potassium t-butoxide to produce the desired allyl alcohol and potassium borohydride. Finally, the palladium complex catalyst reduces the carbonyl group of the starting material, converting it into an aldehyde. Allylboronic acid pinacol ester is commercially available as a white solid, but can also be synthesized from 2-chloro-5-pinacolylborane (pinacol) in high yield using catalytic cross coupling reactions., Application In Synthesis of 72824-04-5

Some low molecular weight alcohols of industrial importance are produced by the addition of water to alkenes. 72824-04-5, formula is C9H17BO2, Ethanol, isopropanol, 2-butanol, and tert-butanol are produced by this general method. Two implementations are employed, the direct and indirect methods. Application In Synthesis of 72824-04-5

Wang, Jie;Zhang, Qingxia;Li, Yao;Liu, Xiangshuai;Li, Xin;Cheng, Jin-Pei research published 《 Bi(OAc)3/chiral phosphoric acid catalyzed enantioselective allylation of isatins》, the research content is summarized as follows. An efficient protocol for construction of chiral 3-allyl-3-hydroxyoxindoles I (R = 4-Cl, 5-Br, 6-F, etc.; R1 = Me, Ph, naphthalen-1-ylmethyl, etc.) via the enantioselective allylation reaction of isatins II and allylboronates CH2=CH(R2)C(R3)(R4)B(-OC(CH3)2C(CH3)2O-) (R2 = R3 = R4 = H, Me) catalyzed by a simple binary acid Bi(OAc)3/chiral phosphoric acid system under mild conditions was disclosed. The synthetic utility of this strategy has been demonstrated through the formal synthesis of ent-CPC-1.

72824-04-5, Allylboronic acid pinacol ester is a useful research compound. Its molecular formula is C9H17BO2 and its molecular weight is 168.04 g/mol. The purity is usually 95%.
Allylboronic acid pinacol ester is an allylation reagent that is used to produce aldehydes from ketones. It reacts with water, yielding the desired product and formaldehyde as a byproduct. The reaction proceeds through a sequence of steps, in which the boronate ester first reacts with water to form an allylboronate ion and hydrogen gas. This intermediate then reacts with potassium t-butoxide to produce the desired allyl alcohol and potassium borohydride. Finally, the palladium complex catalyst reduces the carbonyl group of the starting material, converting it into an aldehyde. Allylboronic acid pinacol ester is commercially available as a white solid, but can also be synthesized from 2-chloro-5-pinacolylborane (pinacol) in high yield using catalytic cross coupling reactions., Application In Synthesis of 72824-04-5

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts